Direct observation of deformation and resistance to damage accumulation during shock loading of stabilized nanocrystalline Cu-Ta alloys
Year: 2024
Type: article
Abstract: Energy absorption by matter is fundamental to natural and man-made processes. However, despite this ubiquity, developing materials capable of withstanding severe energy fluxes without degradation is a significant challenge in materials science and engineering. Despite recent advances in creating alloys resistant to energy fluxes, mitigating the damage caused by the absorption and transfer of mechanical energy remains a critical obstacle in both fundamental science and technological applications. This challenge is especially prominent when the mechanical energy is transferred to the material by shock loading. This study demonstrates a phenomenon in which microstructurally stabilized nanocrystalline Cu-Ta alloys can undergo reversal or nearly complete recovery of the dislocation structure after multiple shock-loading impacts, unlike any other known metallic material. The microstructure of these alloys can withstand repeated shock-wave interactions at pressures up to 12 GPa without any significant microstructural damage or deterioration, demonstrating an extraordinary capacity to be virtually immune to the detrimental effects of shock loading.
Source: Nature Communications
Language: English
Subfield: Materials Chemistry
Field: Materials Science
Domain: Physical Sciences
Open Access status: gold
Estimated APC paid: $6,790
Awards: G201141372, G2517776751, G2744669132, Investigation of fundamental creep behavior and mechanisms in a thermally stable nanocrystalline alloy, G3448357424, G3732666562, DEVELOPMENT OF MULTI-PHYSICS BASED HYBRID MANUFACTURING FOR UNIQUE MICROSTRUCTURE, G5259331294, CHARACTERIZING DYNAMIC RESPONSES OF ADVANCED ENGINEERING MATERIALS, Collaborative Research: Fundamental Investigation of Fatigue Crack Growth Mechanisms in Microstructurally-Stable Nanocrystalline Alloys, G6004478451, G6274897657, G6908681509, G7452299184, G7732170383, G8727049869
OpenAlex ID: W4403684061
